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NCT ID: NCT04343898 Completed - Clinical trials for Coronavirus Infection

Study of the Treatment and Outcomes in Critically Ill Patients With COVID-19

STOP-COVID
Start date: April 1, 2020
Phase:
Study type: Observational

Multicenter observational/registry study of the clinical features and outcomes of critically ill patients with COVID-19.

NCT ID: NCT04344080 Completed - COVID-19 Clinical Trials

Effect of CytoSorb Adsorber on Hemodynamic and Immunological Parameters in Critical Ill Patients With COVID-19

CYTOCOV-19
Start date: April 1, 2020
Phase: N/A
Study type: Interventional

This prospective randomized single Center study investigates to what extent the physical elimination of the inflammatory mediators using the CytoSorb adsorber reduces the morbidity of severely and critically ill patients with Covid-19.

NCT ID: NCT04355442 Completed - COVID-19 Clinical Trials

Evolution of Facial Trauma During COVID Containment Measures

Traumax
Start date: April 1, 2020
Phase:
Study type: Observational

The COVID-19 global pandemic has led to a major professional and social national reorganization: professional because it involves a redeployment of medical staff and material resources, and social because it imposes prolonged containment measures on an entire population. The maxillofacial trauma activity is mainly linked to sports or leisure accidents, fights and road accidents. It seems to appear since the beginning of containment measures a significant drop in maxillofacial trauma activity at the national level, which, if it is demonstrated in a significant way in several French hospital centers, would allow to redeploy the material and human resources related to this activity on sectors in tension due to the pandemic.

NCT ID: NCT04356885 Completed - Mental Disorder Clinical Trials

COVID-19 and Psychotic Symptoms in France

SCHIZOVID-19
Start date: April 1, 2020
Phase:
Study type: Observational

Study the impact of containment related to COVID-19 pandemic on psychotic experiences in the general population in France.

NCT ID: NCT04357418 Completed - COVID-19 Clinical Trials

Psychological Outcome of COVID-19 Lockdown on Psychiatric Hospital Staff and Close Relatives

ICOS
Start date: April 1, 2020
Phase:
Study type: Observational

The purpose of the investigators is to study the psychological impact of the COVID-19 lockdown on the members of the Ville Evrard Hospital staff and their close relatives, and to identify potential lockdown conditions that could increase anxiety, anger and depressive symptoms in this population.

NCT ID: NCT04358510 Completed - COVID-19 Clinical Trials

COVID-19 Mortality Prediction Model

Start date: April 1, 2020
Phase:
Study type: Observational

The objective of this study is to develop and evaluate an algorithm which accurately predicts mortality in COVID-19, pneumonia and mechanically ventilated ICU patients.

NCT ID: NCT04358536 Completed - COVID-19 Clinical Trials

Classification of COVID-19 Infection in Posteroanterior Chest X-rays

Start date: April 1, 2020
Phase:
Study type: Observational

The objective of this study is to assess three configurations of two convolutional deep neural network architectures for the classification of COVID-19 PCX images.

NCT ID: NCT04359498 Completed - Rectal Cancer Clinical Trials

Retrospective Study of Surgical Complications in Patients With Defunctioning Stoma After Low Anterior Resection (LAR)

Start date: April 1, 2020
Phase:
Study type: Observational

This study is being conducted to evaluate the incidence and type of surgical complications occurring in patients who have a defunctioning stoma after LARfor rectal cancer. The data from this retrospective study will be analyzed by the study Sponsor to aid in designing a prospective clinical trial for a new technology that offers a treatment alternative to standard of care defunctioning stoma in patients undergoing LAR for rectal cancer.

NCT ID: NCT04361786 Completed - COVID 19 Clinical Trials

Acral Cutaneous Thrombotic Vasculopathy and Covid-19 Infection

Start date: April 1, 2020
Phase:
Study type: Observational

Spectrum of skin lesions may arise during Covid-19 virus infection. It includes non-specific urticaria, aphtoids lesions, but also acrosyndromes, in particular suggestive of chilblains. Pathological findings showed thrombocytic lymphocytic vasculitis. Chilblains are sometimes associated with Raynaud's phenomenon or acrocyanosis. Dermatological features may present pathophysiological similarities with the inflammatory and respiratory vascular disturbances, which makes all the gravity of this disease, or even with other organs. Indeed, genetic conditions such as familial lupus chilblains, linked to a mutation of TREX1 gene, and SAVI (Sting associated vasculopathy with onset on infancy) have similar clinical presentations. In particular, SAVI associates both acral skin and lung damage, and auto-antibodies. They have recently been identified as type I interferonopathies. Hallmark is interferon signature, i.e. hyperexpression of type I interferon in the blood. The investigators hypothesize Covid-19 may lead to similar skin involvement as in type I interferonopathies. The interferon pathway is involved in anti-viral defense. Covid-19 could cause excessive activation of this pathway. In addition, hyperactivation of the type I interferon pathway leads to modulation of the adaptive immune response. Production of autoantibodies, in particular antiphospholipid antibodies, have thrombogenic properties. Searching for acquired hemostasis disorders and high level of interferon secondary Covid-19 virus infection, could explain this new and misunderstood skin disorder. Then, targeted therapies, both treating and preventing, could be considered.

NCT ID: NCT04362982 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Αn Information System for Symptom Diagnosis and Improvement of Attention Deficit Hyperactivity Disorder (ADHD360)

ADHD360
Start date: April 1, 2020
Phase: N/A
Study type: Interventional

ADHD360 will be an innovative integrated platform for early ADHD diagnosis and intervention against its symptoms. In the core of the platform design there will be a serious game along with a mobile application to monitor behavior and to evaluate the intervention.